Viewing Study NCT05689385



Ignite Creation Date: 2024-05-06 @ 6:30 PM
Last Modification Date: 2024-10-26 @ 2:49 PM
Study NCT ID: NCT05689385
Status: RECRUITING
Last Update Posted: 2023-04-25
First Post: 2023-01-03

Brief Title: eHealth-based Cardiac Rehabilitation in Post-myocardial Infarction Patients
Sponsor: National Taiwan University Hospital
Organization: National Taiwan University Hospital

Study Overview

Official Title: The Effectiveness of eHealth-based Cardiac Rehabilitation in Post-myocardial Infarction Patientsa Randomized Controlled Trial
Status: RECRUITING
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this randomized controlled trial is to compare the effect of eHealth-based cardiac rehabilitation with the effect of usual care on exercise capacity and qualify of life in patients after myocardial infarction
Detailed Description: Cardiac rehabilitation can improve exercise capacity life of quality readmission rate and mortality rate for patients after myocardial infarction International guidelines list cardiac rehabilitation after myocardial infarction as class IA recommendation However low participation rate of cardiac rehabilitation due to barriers such as lacking of time transport or affordability issues is an unsolved problem worldwide

eHealth consisting of telemedicine mobile health and personalized care using wearable devices has the potential to remove the barriers and become an effective model to deliver cardiac rehabilitation Thus we design a randomized controlled trial to compare the effect of a case manager-led eHealth-based cardiac rehabilitation program with usual care on the compliance physical activity quality of life and cardiorespiratory fitness in patients after myocardial infarction

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None